Search results for bdnf

603 hits were found for bdnf

# Family MCID Name MIFTS Score
1
P BPL003 Bipolar Disorder 56 3.062
2
P MJR001 Major Depressive Disorder 68 2.926
3
P HNT016 Huntington Disease 71 2.925
4
DPR016 Depression 63 2.772
5
ANX010 Anxiety 72 2.662
6
MDD011 Mood Disorder 62 2.488
7
P SCH015 Schizophrenia 75 2.453
8
P RTT002 Rett Syndrome 80 2.413
9
P ALZ034 Alzheimer Disease 88 2.399
10
P EPL164 Epilepsy 71 2.376
11
P DMN002 Dementia 67 2.336
12
P ATS364 Autism 65 2.200
13
P BRS047 Breast Cancer 96 2.186
14
ETN001 Eating Disorder 59 2.175
15
P ATT013 Attention Deficit-Hyperactivity Disorder 64 2.154
16
ISC004 Ischemia 60 2.137
17
OBS002 Obsessive-Compulsive Disorder 68 2.131
18
PSY004 Psychotic Disorder 67 2.113
19
STT001 Status Epilepticus 59 2.094
20
P TMP001 Temporal Lobe Epilepsy 50 2.088
21
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.081
22
ANR007 Anorexia Nervosa 63 2.074
23
P MLT020 Multiple Sclerosis 72 2.067
24
BLM002 Bulimia Nervosa 57 2.045
25
SPN186 Spinal Cord Injury 60 2.028
26
SCH012 Schizoaffective Disorder 50 2.003
27
P SNS001 Sensorineural Hearing Loss 61 1.984
28
RLP002 Relapsing-Remitting Multiple Sclerosis 55 1.984
29
P MTR014 Motor Neuron Disease 64 1.973
30
CNT097 Central Hypoventilation Syndrome, Congenital 70 1.963
31
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 49 1.951
32
MNT002 Mental Depression 57 1.947
33
AST005 Asthma 77 1.925
34
SDD001 Sudden Infant Death Syndrome 61 1.925
35
CRB004 Cerebral Artery Occlusion 44 1.901
36
CRT072 Creutzfeldt-Jakob Disease 69 1.893
37
P NRB001 Neuroblastoma 71 1.873
38
ALC007 Alcohol Dependence 66 1.837
39
P PRK057 Parkinson Disease, Late-Onset 76 1.792
40
c ATS007 Autism Spectrum Disorder 67 1.792
41
PST028 Post-Traumatic Stress Disorder 58 1.792
42
P ALC033 Alcohol Use Disorder 58 1.767
43
P SBS003 Substance Abuse 54 1.725
44
END040 Endogenous Depression 54 1.725
45
P PNC025 Panic Disorder 53 1.710
46
P PRS038 Personality Disorder 65 1.676
47
IRR002 Irritable Bowel Syndrome 63 1.676
48
P RTN016 Retinal Degeneration 53 1.676
49
c BPL002 Bipolar I Disorder 49 1.676
50
FBR047 Fibromyalgia 59 1.666
51
P DYS154 Dystonia 65 1.657
52
GNR004 Generalized Anxiety Disorder 56 1.657
53
PRN009 Paranoid Schizophrenia 49 1.657
54
P FRG001 Fragile X Syndrome 68 1.646
55
BRD004 Borderline Personality Disorder 53 1.635
56
c FTL006 Fetal Alcohol Spectrum Disorder 42 1.635
57
CRB037 Cerebral Palsy 68 1.624
58
CNS004 Constipation 57 1.624
59
APH002 Aphasia 57 1.624
60
PST021 Postpartum Depression 50 1.624
61
P OPN001 Open-Angle Glaucoma 49 1.624
62
HRN003 Heroin Dependence 44 1.624
63
P SLP006 Sleep Apnea 69 1.611
64
P DRM053 Dermatitis, Atopic 66 1.611
65
P CRD246 Cardiovascular System Disease 56 1.611
66
DRG003 Drug Dependence 47 1.611
67
CRV043 Cervical Dystonia 45 1.611
68
GLL008 Gilles De La Tourette Syndrome 66 1.598
69
P ANR048 Aniridia 1 63 1.598
70
P CYS018 Cystitis 59 1.598
71
EYD002 Eye Disease 58 1.598
72
c CNT035 Central Nervous System Disease 54 1.598
73
CCN002 Cocaine Abuse 48 1.598
75
P MDL005 Medulloblastoma 77 1.583
76
P OST002 Osteoporosis 73 1.583
77
P INT143 Interstitial Cystitis 61 1.583
78
NRT004 Neuritis 53 1.583
79
P NRC002 Narcolepsy 51 1.583
80
P HYD006 Hydrocephalus 65 1.566
81
P DBT009 Diabetes Mellitus 64 1.566
82
P PRD006 Prader-Willi Syndrome 59 1.566
83
BNG009 Benign Epilepsy with Centrotemporal Spikes 58 1.566
84
P OPT009 Optic Neuritis 56 1.566
85
P NRM002 Normal Pressure Hydrocephalus 56 1.566
86
SBS004 Substance Dependence 48 1.566
87
CNN002 Cannabis Abuse 44 1.566
88
TRN012 Transient Global Amnesia 40 1.566
89
c HYP595 Hypertension, Essential 84 1.545
90
P CNR004 Cone-Rod Dystrophy 2 71 1.545
91
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 1.545
92
SKN016 Skin Disease 63 1.545
93
NTR005 Nutritional Deficiency Disease 61 1.545
94
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.545
95
SNS003 Sensory Peripheral Neuropathy 53 1.545
96
c PRM108 Primary Progressive Multiple Sclerosis 51 1.545
97
MNN009 Meningoencephalitis 49 1.545
98
P ASP001 Asperger Syndrome 48 1.545
99
SPC010 Speech and Communication Disorders 47 1.545
100
DRY001 Dry Eye Syndrome 47 1.545
101
P HRD021 Hereditary Sensory Neuropathy 47 1.545
102
SGM008 Segmental Dystonia 28 1.545
103
TRM010 Traumatic Brain Injury 53 1.421
104
BRN071 Brain Injury 49 1.395
105
ACT084 Acute Stress Disorder 48 1.366
106
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 1.284
107
AMN003 Amnestic Disorder 54 1.267
108
TBC004 Tobacco Addiction 64 1.259
109
STR067 Stroke, Ischemic 80 1.250
110
P SLP005 Sleep Disorder 59 1.240
111
P FTL001 Fetal Alcohol Syndrome 55 1.209
112
NRT001 Neurotic Disorder 52 1.197
113
OCL052 Ocular Dominance 41 1.197
114
c MGR028 Migraine with or Without Aura 1 69 1.185
115
P OPT006 Optic Nerve Disease 57 1.185
116
P PRP019 Peripheral Nervous System Disease 57 1.185
117
FCL014 Focal Epilepsy 54 1.185
118
OCL006 Ocular Hypertension 53 1.185
119
DSS008 Disease of Mental Health 57 1.171
120
P RTN008 Retinitis Pigmentosa 77 1.156
121
c PNS012 Paine Syndrome 61 1.156
122
SCH003 Schizophreniform Disorder 56 1.156
123
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 1.156
124
LPT014 Leptin Deficiency or Dysfunction 73 1.139
125
c EXD008 Exudative Vitreoretinopathy 1 69 1.139
126
AMB002 Amblyopia 50 1.139
127
DYS009 Dysthymic Disorder 48 1.139
128
c ERL020 Early-Onset Schizophrenia 44 1.139
129
TND006 Tendinosis 42 1.139
130
PCK003 Pick Disease of Brain 68 1.119
131
P NRV007 Nervous System Disease 66 1.119
132
P PRV006 Pervasive Developmental Disorder 57 1.119
133
DMY004 Demyelinating Disease 52 1.119
134
SMT006 Somatoform Disorder 51 1.119
135
RTN003 Retinal Ischemia 50 1.119
136
ADR040 Adrenal Gland Pheochromocytoma 46 1.119
137
ATY001 Atypical Depressive Disorder 45 1.119
138
RTR001 Retrograde Amnesia 45 1.119
139
PHB001 Phobic Disorder 41 1.119
140
MLN003 Melancholia 39 1.119
141
DBT081 Diabetic Encephalopathy 36 1.119
142
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 1.093
143
P TTR001 Tetralogy of Fallot 69 1.093
144
DMN031 Dementia, Lewy Body 65 1.093
145
P CHR071 Charcot-Marie-Tooth Disease 64 1.093
146
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 1.093
147
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 56 1.093
148
P AGN002 Agnosia 54 1.093
149
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 54 1.093
150
P ATN002 Autonomic Nervous System Disease 52 1.093
151
CHR073 Choreatic Disease 52 1.093
152
TXC002 Toxic Encephalopathy 52 1.093
153
MSC190 Muscular Disease 51 1.093
154
WRN002 Wernicke-Korsakoff Syndrome 49 1.093
155
LBS001 Lubs X-Linked Mental Retardation Syndrome 49 1.093
156
HYP016 Hypochondriasis 45 1.093
157
SYD002 Sydenham Chorea 44 1.093
158
ADJ001 Adjustment Disorder 41 1.093
159
CRN031 Cranial Nerve Disease 40 1.093
160
P PRP021 Peripheral Nervous System Neoplasm 39 1.093
161
ENC005 Encephalomalacia 38 1.093
162
ANT019 Anterograde Amnesia 37 1.093
163
c CHR087 Chronic Cystitis 35 1.093
164
P CHR084 Chromosomal Disease 32 1.093
165
SPC003 Specific Developmental Disorder 30 1.093
166
c ATM007 Autoimmune Disease of Central Nervous System 30 1.093
167
LMB001 Lumbosacral Plexus Lesion 29 1.093
168
OCC005 Occlusion Precerebral Artery 28 1.093
169
P ATN003 Autonomic Nervous System Neoplasm 27 1.093
170
c DFN257 Deafness, Autosomal Dominant 33 22 1.093
171
c XLN230 X-Linked Monogenic Disease 20 1.093
172
NRV002 Nerve Fibre Bundle Defect 18 1.093
173
c MJR024 Major Affective Disorder 9 41 0.368
174
c MJR022 Major Affective Disorder 8 38 0.368
175
P CHR345 Chronic Pain 50 0.196
176
VSL002 Visual Epilepsy 58 0.162
177
P SZR006 Seizure Disorder 58 0.159
178
HYP066 Hyperglycemia 61 0.139
179
HYP266 Hypoxia 56 0.139
180
P LTR001 Lateral Sclerosis 53 0.139
181
ALL026 Allergic Hypersensitivity Disease 64 0.131
182
P GLM045 Glioma 63 0.131
183
GLL048 Glial Tumor 45 0.127
184
c BRN108 Branchiootic Syndrome 1 61 0.119
185
CRB039 Cerebrovascular Disease 69 0.115
186
VSC002 Vascular Dementia 57 0.115
187
SVR004 Severe Combined Immunodeficiency 73 0.110
188
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.110
189
P MJR007 Major Affective Disorder 1 43 0.106
190
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.101
191
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.101
192
AGN016 Aging 56 0.101
193
TTN003 Tetanus 64 0.095
194
CYT002 Cytokine Deficiency 44 0.095
195
P CLR023 Colorectal Cancer 98 0.090
196
P MCR115 Microvascular Complications of Diabetes 5 66 0.090
197
CRT015 Carotid Artery Occlusion 44 0.090
198
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.090
199
ALL014 Allergic Encephalomyelitis 39 0.090
200
HYP056 Hypoglycemia 66 0.084
201
P MNN013 Meningitis 65 0.084
202
P END044 Endometriosis 62 0.084
203
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.084
204
P MVM001 Movement Disease 61 0.084
205
P BCL017 B-Cell Lymphoma 58 0.084
206
P NRP001 Neuropathy 56 0.084
207
DBT010 Diabetic Neuropathy 55 0.084
208
GLC003 Glucose Intolerance 54 0.084
209
IMP005 Impotence 52 0.084
210
P KDN018 Kidney Disease 70 0.078
211
DWN001 Down Syndrome 70 0.078
212
P HYP086 Hypothyroidism 68 0.078
213
DRM006 Dermatitis 61 0.078
214
P ENC018 Encephalopathy 61 0.078
215
P INF032 Infertility 57 0.078
216
BRN004 Brain Edema 55 0.078
217
c BCT007 Bacterial Meningitis 55 0.078
218
HYP060 Hyperinsulinism 54 0.078
219
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.078
220
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.078
221
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.078
222
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.078
223
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.078
224
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.078
225
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.078
226
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.078
227
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.078
228
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.078
229
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.078
230
SPS057 Spasticity 41 0.078
231
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.071
232
INS024 Insulin-Like Growth Factor I 79 0.071
233
CRV035 Cervical Cancer 76 0.071
234
P RTN024 Retinoblastoma 72 0.071
235
NRM005 Neuromuscular Disease 63 0.071
236
P CRN300 Coronary Heart Disease 1 63 0.071
237
ALL006 Allergic Asthma 56 0.071
238
DYS073 Dysphagia 50 0.071
239
VCC001 Vaccinia 49 0.071
240
HDN002 Head Injury 45 0.071
241
P LNG032 Lung Cancer 97 0.064
242
P HRT032 Heart Disease 75 0.064
243
GLB015 Glioblastoma Multiforme 75 0.064
244
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.064
245
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.064
246
c GLC092 Glaucoma, Primary Open Angle 62 0.064
247
SQM006 Squamous Cell Carcinoma 60 0.064
248
TRD006 Tardive Dyskinesia 55 0.064
249
AVD001 Avoidant Personality Disorder 54 0.064
250
P TRM003 Tremor 53 0.064
251
P MSC003 Muscular Atrophy 52 0.064
252
P AST007 Astrocytoma 50 0.064
253
P OVR082 Overgrowth Syndrome 50 0.064
254
OPT003 Opiate Dependence 50 0.064
255
WTH001 Withdrawal Disorder 48 0.064
256
c SCH079 Schizophrenia 1 48 0.064
257
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.064
259
MYL069 Myeloma, Multiple 85 0.055
260
P BLD134 Bladder Cancer 78 0.055
261
OST012 Osteoarthritis 78 0.055
262
P AMY004 Amyloidosis 70 0.055
263
P CRD119 Cardiac Arrest 67 0.055
264
ALL003 Allergic Rhinitis 67 0.055
265
OST159 Osteogenic Sarcoma 66 0.055
266
c CHR684 Chronic Kidney Disease 66 0.055
267
P HRP006 Herpes Simplex 65 0.055
268
MSC007 Muscle Hypertrophy 63 0.055
269
LPD008 Lipid Metabolism Disorder 62 0.055
270
P PSR002 Psoriasis 62 0.055
271
TRN015 Transient Cerebral Ischemia 62 0.055
272
P ENC004 Encephalitis 61 0.055
273
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.055
274
IRN002 Iron Metabolism Disease 57 0.055
275
P RHN004 Rhinitis 57 0.055
276
CHL014 Cholera 55 0.055
277
P RST001 Restless Legs Syndrome 54 0.055
278
P TCD001 Tic Disorder 54 0.055
279
c FML008 Familial Retinoblastoma 53 0.055
280
P RTN018 Retinal Disease 52 0.055
281
PST011 Pustulosis of Palm and Sole 52 0.055
282
PNG002 Pain Agnosia 51 0.055
283
OPD006 Opioid Addiction 48 0.055
284
HLX001 Helix Syndrome 47 0.055
285
ATN005 Autonomic Dysfunction 47 0.055
286
P MGL013 Megalencephaly 45 0.055
287
P BLP003 Blepharospasm 44 0.055
288
MRP001 Morphine Dependence 41 0.055
289
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 0.055
290
ALX002 Alexithymia 39 0.055
291
48X005 48,xyyy 39 0.055
292
CHR178 Chromosomal Triplication 35 0.055
293
PPL052 Papillomatosis, Confluent and Reticulated 34 0.055
294
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.055
295
c MJR003 Major Affective Disorder 6 33 0.055
296
c MJR006 Major Affective Disorder 5 33 0.055
297
P HPT023 Hepatocellular Carcinoma 100 0.045
298
P PRS040 Prostate Cancer 97 0.045
299
P OVR042 Ovarian Cancer 89 0.045
300
c SYS001 Systemic Lupus Erythematosus 86 0.045
301
P MYC007 Myocardial Infarction 70 0.045
302
ADN011 Adenoid Cystic Carcinoma 70 0.045
303
P FRN006 Frontotemporal Dementia 70 0.045
304
P MPL001 Maple Syrup Urine Disease 69 0.045
305
c MCR129 Microvascular Complications of Diabetes 1 66 0.045
306
CHG001 Chagas Disease 66 0.045
307
ATH013 Atherosclerosis Susceptibility 66 0.045
308
c SML038 Small Cell Cancer of the Lung 65 0.045
309
P MYP004 Myopathy 64 0.045
310
KHL003 Kohlschutter-Tonz Syndrome 64 0.045
311
P PRD008 Periodontitis 62 0.045
312
CLT003 Colitis 62 0.045
313
c WLM018 Wilms Tumor 5 62 0.045
314
P HYP750 Hypertriglyceridemia, Familial 61 0.045
315
NRL005 Neurilemmoma 60 0.045
316
HPT019 Hepatic Encephalopathy 60 0.045
317
INS001 Insulinoma 60 0.045
318
ORL011 Oral Cancer 60 0.045
319
THY029 Thyroid Carcinoma 59 0.045
320
P SPN309 Spinocerebellar Ataxia 6 59 0.045
321
PRT058 Pure Autonomic Failure 59 0.045
322
P BND020 Bone Disease 59 0.045
323
GST045 Gastroenteritis 59 0.045
324
P TYR004 Tyrosinemia 58 0.045
325
END030 End Stage Renal Failure 58 0.045
326
P HDC001 Headache 57 0.045
327
P BNC003 Bone Cancer 57 0.045
328
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.045
329
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.045
330
P DRR001 Diarrhea 57 0.045
331
PLC005 Placental Insufficiency 57 0.045
332
TRN018 Transitional Cell Carcinoma 56 0.045
333
c ACT075 Acute Myocardial Infarction 56 0.045
334
ACS001 Acoustic Neuroma 56 0.045
335
P PLY019 Polyneuropathy 56 0.045
336
INT007 Intermediate Coronary Syndrome 55 0.045
337
SMT008 Smith-Magenis Syndrome 55 0.045
338
HMS001 Hemosiderosis 54 0.045
339
AMN001 Amenorrhea 54 0.045
340
PRP016 Paraplegia 53 0.045
341
PTH003 Pathologic Nystagmus 51 0.045
342
OCL069 Ocular Motor Apraxia 51 0.045
343
CND002 Conduct Disorder 51 0.045
344
P FBR031 Febrile Seizures 51 0.045
345
LRN003 Learning Disability 49 0.045
346
BNR002 Bone Resorption Disease 48 0.045
347
PTH002 Pathological Gambling 48 0.045
348
CCN001 Cocaine Dependence 48 0.045
349
SCL003 Social Phobia 48 0.045
350
SXL003 Sexual Disorder 48 0.045
351
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.045
352
RTN023 Retinitis 46 0.045
353
c TYR013 Tyrosinemia, Type Ii 46 0.045
354
CNV002 Conversion Disorder 45 0.045
355
c MLG068 Malignant Glioma 45 0.045
356
SBC016 Subacute Delirium 44 0.045
357
c PCH010 Pachyonychia Congenita 3 43 0.045
358
PNM013 Pneumococcal Meningitis 43 0.045
359
HPT004 Hepatic Coma 43 0.045
360
ORL015 Oral Squamous Cell Carcinoma 43 0.045
361
PLY068 Polysubstance Abuse 43 0.045
362
NRR001 Neuroretinitis 43 0.045
363
MYF002 Myofascial Pain Syndrome 42 0.045
364
PHY002 Physical Disorder 42 0.045
365
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.045
366
RST023 Resting Heart Rate, Variation in 41 0.045
367
P HYP263 Hypersomnia 41 0.045
368
c MCR112 Microvascular Complications of Diabetes 2 41 0.045
369
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.045
370
TRN007 Transsexualism 40 0.045
372
SCH011 Schizotypal Personality Disorder 39 0.045
373
SPP007 Suppression Amblyopia 39 0.045
374
DPR002 Depersonalization Disorder 38 0.045
375
HYP835 Hypothalamic Obesity 38 0.045
376
BRN018 Borna Disease 35 0.045
377
HYP679 Hypoglossia-Hypodactylia 34 0.045
378
PLY150 Polykaryocytosis Inducer 31 0.045
379
WLM019 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome 17 0.045
380
P GST053 Gastric Cancer 83 0.032
381
NRL016 Neural Tube Defects 82 0.032
382
P RHM011 Rheumatoid Arthritis 80 0.032
383
c LKM071 Leukemia, Chronic Lymphocytic 79 0.032
384
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.032
385
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.032
386
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.032
387
DFC004 Deficiency Anemia 75 0.032
388
END057 Endometrial Cancer 74 0.032
389
c MNN043 Meningioma, Familial 74 0.032
390
ACR006 Aceruloplasminemia 73 0.032
391
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.032
392
SCK003 Sickle Cell Anemia 72 0.032
393
c HYP836 Hypercholesterolemia, Familial, 1 72 0.032
394
P PHC003 Pheochromocytoma 71 0.032
395
P TBR001 Tuberous Sclerosis 70 0.032
396
P SYS005 Systemic Scleroderma 70 0.032
397
P LVR013 Liver Disease 68 0.032
398
P LYM118 Lymphoma 68 0.032
399
P PLM037 Pulmonary Hypertension 68 0.032
400
c NMN015 Niemann-Pick Disease, Type C1 68 0.032
401
P OLG002 Oligodendroglioma 67 0.032
402
GRG001 Greig Cephalopolysyndactyly Syndrome 67 0.032
403
P LPR021 Leprosy 3 67 0.032
404
P LKM002 Leukemia 66 0.032
405
c FML001 Familial Atrial Fibrillation 66 0.032
406
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.032
407
P ATR011 Atrial Fibrillation 66 0.032
408
P BRD002 Bardet-Biedl Syndrome 66 0.032
409
ANG054 Angina Pectoris 66 0.032
410
c HRD010 Hereditary Spastic Paraplegia 66 0.032
411
LNG039 Lung Squamous Cell Carcinoma 65 0.032
412
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.032
413
PRT037 Pertussis 65 0.032
414
P TRN020 Turner Syndrome 65 0.032
415
P THY023 Thymoma 65 0.032
416
APN008 Apnea, Obstructive Sleep 65 0.032
417
P KLL001 Kallmann Syndrome 64 0.032
418
P ADN016 Adenocarcinoma 64 0.032
419
P SPN046 Spinal Muscular Atrophy 64 0.032
420
P VSC007 Vascular Disease 63 0.032
421
IDP011 Idiopathic Interstitial Pneumonia 63 0.032
422
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 63 0.032
423
c PRC016 Pre-Eclampsia 63 0.032
424
LVR012 Liver Cirrhosis 63 0.032
425
P CRN018 Coronary Artery Anomaly 63 0.032
426
c ACT068 Acute Cystitis 63 0.032
427
ACT119 Acute Promyelocytic Leukemia 63 0.032
428
c HPT003 Hepatitis a 63 0.032
429
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.032
430
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.032
431
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.032
432
c FNC043 Fanconi Anemia, Complementation Group E 62 0.032
433
LSC001 Lesch-Nyhan Syndrome 62 0.032
434
MNN042 Meningioma, Radiation-Induced 62 0.032
435
P PLM036 Pulmonary Fibrosis 61 0.032
436
FTT001 Fatty Liver Disease 61 0.032
437
P LPS004 Lupus Erythematosus 61 0.032
438
P KDN017 Kidney Cancer 61 0.032
439
P PNC044 Pancreatitis 61 0.032
440
ATM095 Autoimmune Disease 61 0.032
441
P NRM001 Neuromyelitis Optica 60 0.032
442
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.032
443
DPH001 Diphtheria 60 0.032
444
TRG002 Trigeminal Neuralgia 60 0.032
445
P NMN002 Niemann-Pick Disease 60 0.032
446
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.032
447
SPP011 Suppression of Tumorigenicity 12 59 0.032
448
HLC007 Helicobacter Pylori Infection 59 0.032
449
IRN001 Iron Deficiency Anemia 58 0.032
450
P FCL005 Focal Segmental Glomerulosclerosis 58 0.032
451
CHL067 Cholecystitis 58 0.032
452
CRV038 Cervical Squamous Cell Carcinoma 58 0.032
453
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.032
454
c ACT073 Acute Leukemia 58 0.032
455
RBS001 Rabies 58 0.032
456
c DWL002 Dowling-Degos Disease 1 58 0.032
457
BLR008 Bilirubin Metabolic Disorder 57 0.032
458
GST033 Gestational Diabetes 57 0.032
459
P PRN023 Prion Disease 57 0.032
460
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.032
461
DNT005 Dentatorubral-Pallidoluysian Atrophy 57 0.032
462
c ESS001 Essential Tremor 56 0.032
463
PRS047 Prostatitis 56 0.032
464
P STR020 Strabismus 56 0.032
465
THR024 Thrombosis 56 0.032
466
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.032
467
P CHN012 Chondrosarcoma 56 0.032
468
P FBR017 Fibrosarcoma 56 0.032
469
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.032
470
PLS011 Plasmacytoma 56 0.032
471
P PLY011 Polycystic Ovary Syndrome 56 0.032
472
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.032
473
RHM027 Rheumatic Disease 56 0.032
474
c SVR001 Severe Acute Respiratory Syndrome 55 0.032
475
P HYP076 Hyperthyroidism 55 0.032
476
c NPH055 Nephrotic Syndrome, Type 1 55 0.032
477
NRN004 Neuroendocrine Tumor 55 0.032
478
PLM010 Pulmonary Edema 55 0.032
479
P LYM031 Lymphocytic Leukemia 55 0.032
480
NRG002 Neurogenic Bladder 54 0.032
481
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 54 0.032
482
c THY107 Thymoma, Familial 54 0.032
483
BRN045 Brunner Syndrome 53 0.032
484
CLR030 Clear Cell Renal Cell Carcinoma 53 0.032
485
P HYP730 Hypogonadotropic Hypogonadism 53 0.032
486
HMC014 Homocysteinemia 53 0.032
487
ART140 Arteries, Anomalies of 53 0.032
488
GNG002 Ganglioneuroma 53 0.032
489
c MCR113 Microvascular Complications of Diabetes 3 52 0.032
490
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.032
491
c SPN294 Spinocerebellar Ataxia 1 52 0.032
492
PRS045 Prostatic Hypertrophy 52 0.032
493
PRV004 Periventricular Leukomalacia 51 0.032
494
c VRL010 Viral Hepatitis 51 0.032
495
PRS021 Prostatic Adenoma 51 0.032
496
c VRL007 Viral Encephalitis 51 0.032
497
NRM004 Neuroma 51 0.032
498
CLR109 Colorectal Adenocarcinoma 50 0.032
499
DBT004 Diabetic Polyneuropathy 50 0.032
500
P MGR003 Migraine with Aura 50 0.032
501
HYP080 Hypogonadism 50 0.032
502
47X002 47,xyy 49 0.032
503
PRS129 Prostatic Hyperplasia, Benign 49 0.032
504
KBG001 Kbg Syndrome 49 0.032
505
ENT004 Enthesopathy 48 0.032
506
c NPH049 Nephrotic Syndrome, Type 2 48 0.032
507
HYP043 Hyperandrogenism 48 0.032
508
P MGR001 Migraine Without Aura 48 0.032
509
ATX019 Ataxia with Vitamin E Deficiency 48 0.032
510
P INN002 Inner Ear Disease 48 0.032
511
DGN001 Degenerative Disc Disease 48 0.032
512
SMT001 Somatization Disorder 48 0.032
513
ANV001 Anovulation 47 0.032
514
c MCR120 Microvascular Complications of Diabetes 7 47 0.032
515
SPN021 Spinal Meningioma 47 0.032
516
NRN001 Neuroendocrine Carcinoma 47 0.032
517
PNC013 Pancreatic Ductal Carcinoma 47 0.032
518
SMN008 Semantic Dementia 47 0.032
519
RYN005 Raynaud Phenomenon 46 0.032
520
CHR074 Choriocarcinoma 46 0.032
521
P VTR007 Vitreoretinopathy 46 0.032
522
OPD001 Opioid Abuse 45 0.032
523
P SXD002 Sex Development Disorder 45 0.032
524
ASP004 Asphyxia Neonatorum 45 0.032
525
c NNN011 Noonan Syndrome 4 44 0.032
526
AGR002 Agoraphobia 44 0.032
527
c BRD016 Bardet-Biedl Syndrome 4 44 0.032
528
P BRB001 Beriberi 44 0.032
529
LRY022 Laryngoonychocutaneous Syndrome 44 0.032
530
ATN004 Autonomic Neuropathy 44 0.032
531
BCK003 Background Diabetic Retinopathy 44 0.032
532
LRG014 Large Cell Neuroendocrine Carcinoma 44 0.032
533
GLL017 Gallbladder Adenocarcinoma 43 0.032
534
P CLS010 Cluster Headache 43 0.032
535
FCL022 Focal Dystonia 42 0.032
536
LWC001 Low Compliance Bladder 42 0.032
537
PST053 Postherpetic Neuralgia 42 0.032
538
ANX004 Anoxia 42 0.032
539
P HYP265 Hypotonia 42 0.032
540
PHH001 Phaeohyphomycosis 42 0.032
541
FTL021 Fetal Macrosomia 42 0.032
542
DBT002 Diabetic Autonomic Neuropathy 41 0.032
543
c MCR130 Microvascular Complications of Diabetes 6 41 0.032
544
c MCR133 Microvascular Complications of Diabetes 4 41 0.032
545
P RRH023 Rare Hereditary Hemochromatosis 41 0.032
546
GND002 Gender Identity Disorder 41 0.032
547
RDN001 Reading Disorder 40 0.032
548
DNT006 Dental Pulp Necrosis 40 0.032
549
HYP064 Hypogonadotropism 40 0.032
550
c NNN021 Noonan Syndrome 8 40 0.032
551
CLP005 Ciliopathy 40 0.032
552
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.032
553
LKP003 Leukoplakia 39 0.032
554
PRM020 Premenstrual Tension 39 0.032
555
P DYS021 Dysautonomia 39 0.032
556
ORL012 Oral Leukoplakia 39 0.032
557
MCH006 Mechanical Strabismus 39 0.032
558
MNN017 Mononeuropathy 39 0.032
559
c CHR682 Chronic Bilirubin Encephalopathy 38 0.032
560
P CRB088 Cerebral Atrophy 38 0.032
561
c ATM075 Autoimmune Encephalitis 38 0.032
562
SCR001 Secretory Meningioma 37 0.032
563
P FML187 Familial Hypertension 37 0.032
564
PCD001 Pica Disease 37 0.032
565
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.032
566
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.032
567
HRW001 Hair Whorl 36 0.032
568
c 46X055 46,xy Sex Reversal 3 35 0.032
569
c MJR008 Major Affective Disorder 2 34 0.032
570
HNS001 Hansen's Disease 34 0.032
571
NNT024 Neonatal Stroke 34 0.032
572
GNT167 Genetic Obesity 34 0.032
573
c SCH087 Schizophrenia 18 34 0.032
574
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.032
575
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.032
576
c MJR023 Major Affective Disorder 7 33 0.032
577
IDP031 Idiopathic Hypersomnia 32 0.032
578
ISL011 Isolated Aniridia 32 0.032
579
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.032
580
c NRM008 Neuromyelitis Optica Spectrum Disorder 31 0.032
581
PLM038 Pulmonary Large Cell Neuroendocrine Carcinoma 31 0.032
582
CHL078 Childhood-Onset Schizophrenia 31 0.032
583
MNN024 Meningitis and Encephalitis 29 0.032
584
SYN116 Syndromic Obesity 29 0.032
585
c MJR004 Major Affective Disorder 4 28 0.032
587
ARG004 Argyria 28 0.032
588
OTM001 Otomycosis 28 0.032
589
P FML340 Familial Episodic Pain Syndrome 27 0.032
590
c ERL012 Early-Onset Glaucoma 27 0.032
591
CHL079 Children's Interstitial Lung Disease 27 0.032
592
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 27 0.032
593
LSN001 Lesion of Sciatic Nerve 26 0.032
594
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.032
596
DSC013 Discrimination, Two-Point, Reduction in 23 0.032
597
c SYN140 Syndrome with 46,xy Disorder of Sex Development 23 0.032
598
PST047 Post-Traumatic Epilepsy 22 0.032
599
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.032
600
c SCH061 Schizophrenia 16 21 0.032
601
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.032
602
SPN092 Spinal Shock 19 0.032
603
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.032
Content
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